Taritla Sidhartha, Kumari Madhuree, Kamat Siya, Bhat Sarita G, Jayabaskaran C
Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Department of Biotechnology, Cochin University of Science and Technology, Kochi, India.
Front Pharmacol. 2021 Apr 26;12:542891. doi: 10.3389/fphar.2021.542891. eCollection 2021.
The endophytic fungal community in the marine ecosystem has been demonstrated to be relevant source of novel and pharmacologically active secondary metabolites. The current study focused on the evaluation of cytotoxic and apoptosis induction potential in the culture extracts of endophytic fungi associated with , a marine brown alga. The cytotoxicity of the four marine endophytes, sp., , , and , was evaluated by the MTT assay on HeLa cells. Further, several physicochemical parameters, including growth curve, culture media, and organic solvents, were optimized for enhanced cytotoxic activity of the selected extract. The sp. ethyl acetate extract (ASE) showed maximum cytotoxicity on multiple cancer cell lines. Chemical investigation of the metabolites by gas chromatography-mass spectroscopy (GC-MS) showed the presence of several compounds, including quinoline, indole, 2,4-bis(1,1-dimethylethyl) phenol, and hexadecenoic acid, known to be cytotoxic in ASE. The ASE was then tested for cytotoxicity on a panel of six human cancer cell lines, namely, HeLa (cervical adenocarcinoma), MCF-7 (breast adenocarcinoma), Hep G2 (hepatocellular carcinoma), A-549 (lung carcinoma), A-431 (skin/epidermis carcinoma), and LN-229 (glioblastoma). HeLa cells were most vulnerable to ASE treatment with an IC value of 24 ± 2 μg/ml. The mechanism of cytotoxicity exhibited by the ASE was further investigated on Hela cells. The results showed that the ASE was capable of inducing apoptosis in HeLa cells through production of reactive oxygen species, depolarization of mitochondrial membrane, and activation of the caspase-3 pathway, which shows a possible activation of the intrinsic apoptosis pathway. It also arrested the HeLa cells at the G2/M phase of the cell cycle, eventually leading to apoptosis. Through this study, we add to the knowledge about the marine algae associated with fungal endophytes and report its potential for purifying specific compounds responsible for cytotoxicity.
海洋生态系统中的内生真菌群落已被证明是新型和具有药理活性的次生代谢产物的重要来源。当前的研究聚焦于评估与一种海洋褐藻相关的内生真菌培养提取物的细胞毒性和诱导凋亡的潜力。通过MTT法在HeLa细胞上评估了四种海洋内生菌,即 sp.、 、 和 的细胞毒性。此外,还对包括生长曲线、培养基和有机溶剂在内的几个理化参数进行了优化,以增强所选提取物的细胞毒性活性。 sp.的乙酸乙酯提取物(ASE)对多种癌细胞系表现出最大的细胞毒性。通过气相色谱 - 质谱联用(GC - MS)对代谢产物进行化学研究表明,ASE中存在几种化合物,包括喹啉、吲哚、2,4 - 双(1,1 - 二甲基乙基)苯酚和十六碳烯酸,已知这些化合物具有细胞毒性。然后在一组六种人类癌细胞系上测试了ASE的细胞毒性,这六种细胞系分别是HeLa(宫颈腺癌)、MCF - 7(乳腺腺癌)、Hep G2(肝细胞癌)、A - 549(肺癌)、A - 431(皮肤/表皮癌)和LN - 229(胶质母细胞瘤)。HeLa细胞对ASE处理最为敏感,IC值为24 ± 2 μg/ml。在HeLa细胞上进一步研究了ASE表现出的细胞毒性机制。结果表明,ASE能够通过产生活性氧、线粒体膜去极化和激活caspase - 3途径诱导HeLa细胞凋亡,这表明可能激活了内源性凋亡途径。它还使HeLa细胞停滞在细胞周期的G2/M期,最终导致细胞凋亡。通过这项研究,我们增加了对与真菌内生菌相关的海藻的了解,并报告了其纯化负责细胞毒性的特定化合物的潜力。